Device recall
Z-2433-2019: Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
FDA device recall · Class II · GETINGE US SALES LLC
Key facts
| Recall number (Z-number) | Z-2433-2019 |
|---|---|
| Recall event | 83468 |
| Product | Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems. |
| Product code | BSF |
| Recalling firm | GETINGE US SALES LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 26, 2020 |
| FEI number | 3012092534 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database